Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Chlorotrimethylsilane → 1-{2-[(Trimethylsilyl)oxy]ethyl}-1H-pyrrole-2,5-dione
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Chlorotrimethylsilane | HCID 6397 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | N-(2-Hydroxyethyl)maleimide | HCID 458487 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 1-{2-[(Trimethylsilyl)oxy]ethyl}-1H-pyrrole-2,5-dione | HCID 21829816 | 100% |
반응 단계
To a solution of N-(2-hydroxyethyl)maleimide (0.2 g, 1.41 mmol) in dry dichloromethane (10 ml) and triethylamine (0.22 ml, 1.57 mmol) at 0° C. was added chlorotrimethylsilane (TMS-C1, 0.2 ml, 1.57 mmol). After stirring for 1 hour at room temperature, TLC analysis (ethyl acetate/petroleum ether 1:1) indicated one spot (Rf=0.67). Solvent was removed in vacuo and the residue was dissolved in dichloromethane and filtered through a small silica gel column eluting with dichloromethane. The fractions containing product were pooled and evaporated in vacuo to afford N-(2-trimethylsiloxyethyl)-maleimide (formula H) as colorless flakes (0.3 g; 100% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05763196 |
| 출처 데이터셋 | uspto-grants-1998_06 |
| ORD ID | ord-6c0348c64c004757806113937ab54340 |
| 출처 메모 | uspto-grants-1998_06 |